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R Scholte

Showing results (41-50 of 83) with videos related to

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Laboratory Investigation; a Journal of Technical Methods and Pathology|August 15, 2001
Immunological phenotyping of fibroblast cultures from patients with a mitochondrial respiratory chain deficitS L Williams, H R Scholte, R G Gray, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Vitamin-responsive complex I deficiency in a myopathic patient with increased activity of the terminal respiratory chain and lactic acidosisH D Bakker, H R Scholte, J A Jeneson, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Neonatal cardiomyopathy and lactic acidosis responsive to thiamineH D Bakker, H R Scholte, I E Luyt-Houwen, et al.
Bulletin of the Menninger Clinic|May 30, 2014
Association between level of personality organization as assessed with theory-driven profiles of the Dutch Short Form of the MMPI and outcome of inpatient treatment for personality disorderWubbo R Scholte, Elisabeth H M Eurelings-Bontekoe, Bea G Tiemens, et al.
British Journal of Industrial Medicine|July 1, 1993
Melanoma and occupation: results of a case-control study in The NetherlandsP J Nelemans, R Scholte, H Groenendal, et al.
Biochimica Et Biophysica Acta|May 24, 1995
Riboflavin-responsive complex I deficiencyH R Scholte, H F Busch, H D Bakker, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cellsH R Scholte, H F Busch, I E Luyt-Houwen, et al.
Neuropediatrics|November 1, 1986
Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidaseA M Roodhooft, K J Van Acker, J J Martin, et al.
The Journal of Pediatrics|May 1, 1996
Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver diseaseH D Bakker, H R Scholte, K P Dingemans, et al.
Wiener Klinische Wochenschrift|January 6, 1989
Carnitine deficiency, mitochondrial dysfunction and the heart. Identical defect of oxidative phosphorylation in muscle mitochondria in cardiomyopathy due to carnitine loss and in Duchenne muscular dystrophyH R Scholte, R Rodrigues Pereira, H F Busch, et al.
Pageof 9

Showing results (41-50 of 83) with videos related to

Sort By:
Pageof 9
Laboratory Investigation; a Journal of Technical Methods and Pathology|August 15, 2001
Immunological phenotyping of fibroblast cultures from patients with a mitochondrial respiratory chain deficitS L Williams, H R Scholte, R G Gray, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Vitamin-responsive complex I deficiency in a myopathic patient with increased activity of the terminal respiratory chain and lactic acidosisH D Bakker, H R Scholte, J A Jeneson, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Neonatal cardiomyopathy and lactic acidosis responsive to thiamineH D Bakker, H R Scholte, I E Luyt-Houwen, et al.
Bulletin of the Menninger Clinic|May 30, 2014
Association between level of personality organization as assessed with theory-driven profiles of the Dutch Short Form of the MMPI and outcome of inpatient treatment for personality disorderWubbo R Scholte, Elisabeth H M Eurelings-Bontekoe, Bea G Tiemens, et al.
British Journal of Industrial Medicine|July 1, 1993
Melanoma and occupation: results of a case-control study in The NetherlandsP J Nelemans, R Scholte, H Groenendal, et al.
Biochimica Et Biophysica Acta|May 24, 1995
Riboflavin-responsive complex I deficiencyH R Scholte, H F Busch, H D Bakker, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cellsH R Scholte, H F Busch, I E Luyt-Houwen, et al.
Neuropediatrics|November 1, 1986
Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidaseA M Roodhooft, K J Van Acker, J J Martin, et al.
The Journal of Pediatrics|May 1, 1996
Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver diseaseH D Bakker, H R Scholte, K P Dingemans, et al.
Wiener Klinische Wochenschrift|January 6, 1989
Carnitine deficiency, mitochondrial dysfunction and the heart. Identical defect of oxidative phosphorylation in muscle mitochondria in cardiomyopathy due to carnitine loss and in Duchenne muscular dystrophyH R Scholte, R Rodrigues Pereira, H F Busch, et al.
Pageof 9